ChemicalBook Product Catalog Chemical Reagents Organic reagents Boric acid 4-Ethoxycarbonylphenylboronic acid

4-Ethoxycarbonylphenylboronic acid

4-Ethoxycarbonylphenylboronic acid Basic information
Product Name:4-Ethoxycarbonylphenylboronic acid
Synonyms:Ethyl 4-Boronobenzoat;4-Borono-benzoic Acid 1-Ethyl Ester;p-Borono-benzoic Acid 1-Ethyl Ester;4-(Ethoxycarbonyl)Phenylboroni;4-CARBETHOXY-PHENYL-BORONIC ACID;4-ETHOXYCARBONYLPHENYLBORONIC ACID 98%;Benzoic acid, 4-borono-, 1-ethyl ester;4-Ethoxycarbonylphenylboronic acid, 97% 1GR
CAS:4334-88-7
MF:C9H11BO4
MW:193.99
EINECS:206-141-6
Product Categories:Aryl Boronic Acids;Boronic Acids and Derivatives;Chemical Synthesis;Monosubstituted Aryl Boronic Acids;Organometallic Reagents;Substituted Boronic Acids;Boronic acids;Aryl;Organoborons;Aromatics Compounds;Boronic acid;Aromatics;Boron Derivatives;blocks;BoronicAcids;Carboxes;Boronate Ester;Potassium Trifluoroborate
Mol File:4334-88-7.mol
4-Ethoxycarbonylphenylboronic acid Structure
4-Ethoxycarbonylphenylboronic acid Chemical Properties
Melting point 135 °C (dec.) (lit.)
Boiling point 355.5±44.0 °C(Predicted)
density 1.21±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility soluble in Methanol
pka7.69±0.10(Predicted)
form Powder
color White to off-white
InChIKeyZLNFACCFYUFTLD-UHFFFAOYSA-N
CAS DataBase Reference4334-88-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,T
Risk Statements 36/37/38-26-22
Safety Statements 37/39-26-45-36/37-28
WGK Germany 3
TSCA No
HazardClass IRRITANT
HS Code 29163990
MSDS Information
ProviderLanguage
ACROS English
4-Ethoxycarbonylphenylboronic acid Usage And Synthesis
Chemical Propertieswhite to off-white powder
Uses4-(Ethoxycarbonyl)benzeneboronic acid is used as a reactant involved in oxidative hydroxylation for the preparation of phenols, homolytic aromatic substitution, cross-coupling with α-bromocarbonyl compounds, Suzuki-coupling reaction with quinoline carboxylates, trifluoromethylation and carbometalation of ynamides.
Usessuzuki reaction
UsesReactant involved in:• ;Oxidative hydroxylation for the preparation of phenols1• ;Homolytic aromatic substitution2• ;Cross-coupling with α-bromocarbonyl compounds3• ;Suzuki-coupling reaction with quinoline carboxylates4• ;Trifluoromethylation5• ;Carbometalation of ynamides6
4-Ethoxycarbonylphenylboronic acid Preparation Products And Raw materials
Preparation ProductsMomelotinib-->ETHYL 4-(5-FORMYL-2-FURYL)BENZOATE-->4,6-Di(4-carboxyphenyl)pyrimidine-->ethyl 4-(2-chloropyriMidin-4-yl)benzoate
3-FLUORO-5-ETHOXYCARBONYLPHENYLBORONIC ACID Ethopabate 4-Ethoxycarbonylphenylboronic acid 4-ETHOXYCARBONYLPHENYLBORONIC ACID, PINACOL ESTER 3-Amino-5-ethoxycarbonylphenylboronic acid N-Carbobenzyloxyglycine M-ETHOXYCARBONYLPHENYLBORONIC ACID,3-ETHOXYCARBONYLPHENYLBORONIC ACID Phenylboronic acid 2-FLUORO-4-ETHOXYCARBONYLPHENYLBORONIC ACID 2-ETHOXYCARBONYLPHENYLBORONIC ACID,O-ETHOXYCARBONYLPHENYLBORONIC ACID Phenoxybenzamine hydrochloride 4-Chloro-3-(ethoxycarbonyl)phenylboronic acid 2-Amino-4-ethoxycarbonylphenylboronic acid, HCl 3-ETHOXYCARBONYLPHENYLBORONIC ACID, PINACOL ESTER Tamoxifen 2-ETHOXYCARBONYLPHENYLBORONIC ACID, PINACOL ESTER 2-Phenoxyethanol
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